Antibiotics

8

Review clinical trials related to Antibiotics. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Antibiotics as Adjuncts to Periodontal Therapy:Pharmacokinetic Considerations and Dosing Strategies

Periodontitits is a bacteria induced inflammatory disease that destroys the supporting tissues of the tooth and leads to tooth loss. Treatment consists mainly of the mechanical cleaning of the tooth surfaces in order to remove the bacterial deposits (plaque and calculus). This procedure can reduce the level of pathogenic bacteria but it can not eradicate them. In severe cases, for the complete resolution of the disease, the elimantion of certain species of bacteria is needed. In order to achieve that, the combination of different regimens of antibiotics adjunctive to the mechanical treatment has been proposed. However, dosage and duration of antimicrobial therapy should be optimal and not excessive as issues may arise related to increased antimicrobial resistance in the population and the individual due to habitual prescription of wide-spectrum antibiotic regimens, horizontal gene transfer and genetic mutation. In the present study, in an effort to optimize the dosage and duration of the antimicrobial regimen, we will determine the pharmacokinetics (PK) and pharmacodynamic (PD) properties of the MET-AMO combination and of AZI in Gingival Crevicular Fluid (GCF), saliva and serum in severe periodontitis patients during and after either a 3-day or a 7-day course of treatment.

Participants needed: 45
Trial details
Phase: Phase 4Age: 18-80Biological sex: AllType: InterventionalSponsor: University of Geneva, SwitzerlandUpdated: Apr 29, 2026Locations: 1
Eligibility criteria

Informed Consent as documented by signature [+2]

Persons with systemic illnesses (uncontrolled diabetes mellitus, cancer, human i... [+9]

Status: Recruiting

Antibiotic Prophylaxis for Ureteroscopy With a Negative Pressure Suction Sheath

This study, as a prospective, randomized, controlled, non-inferiority, international multicenter clinical trial, aims to evaluate whether a strategy of no antimicrobial prophylaxis is non-inferior to the traditional single-dose prophylaxis regimen in patients with a low risk of infection undergoing single-use flexible ureteroscopic lithotripsy combined with a flexible negative-pressure suction sheath. It is anticipated that this will have a substantial impact on infection prevention strategies in urological surgery.

Participants needed: 500
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Shanghai General Hospital, Shanghai Jiao Tong University School of MedicineUpdated: Apr 23, 2026Locations: 1
Eligibility criteria

Age 18-75 years. [+6]

Pregnant or lactating women. [+17]

Status: Not yet recruiting

British Columbia Prescriber Feedback Program - Antimicrobial Resistance

The goal of this study is to evaluate an educational intervention that aims to reduce the number of unnecessary antibiotics prescribed by family physicians and nurse practitioners in British Columbia, Canada. The intervention materials include a confidential personalized prescribing "portrait" and an evidence-based educational summary (therapeutics letter), accompanied by an introduction letter. The main research questions are: 1. Will the intervention lead to a reduction in the overall number of antibiotics prescriptions started? 2. Will the intervention lead to a reduction in the proportion of antibiotics prescribed that are likely unnecessary, especially prescriptions for upper respiratory tract infections, acute bronchitis, acute sinusitis? Researchers will conduct an intervention study with family physicians and nurse practitioners in British Columbia, Canada. Participant clinicians will be randomly assigned to one of two groups. The Early Group will consist of 80% of the participants and will receive the intervention (prescribing portrait, evidence summary, and introduction letter) at the start of the study. The Delayed Group will consist of 20% of participants and will receive the intervention about nine months later. This study design allows most practitioners to receive the intervention early while still allowing time to compare the two groups to assess the impact. To estimate the impact of the intervention, researchers will use administrative health data to compare the prescribing of the Early Group with prescribing of the Delayed Group.

Participants needed: 7,626
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of British ColumbiaUpdated: Feb 24, 2026Locations: 1
Eligibility criteria

A valid MSP billing number; [+2]

Previously opted out of the Therapeutics Initiative Portrait program [+4]

Status: Recruiting

Researchers At UC San Diego Are Learning About the Benefits of Human Milk and How It Influences Infant and Child Health

The purpose of the UCSD Human Milk Biorepository is to establish and maintain a repository of breast milk samples that can be used to learn more about how breast milk influences infant and child health.

Participants needed: 5,000
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: University of California, San DiegoUpdated: Jan 31, 2025Locations: 1
Eligibility criteria

Women who are 18 years old or older [+2]

Women under 18 years old

Status: Recruiting

Does Additional Use of Preoperative Azithromycin Decrease Posthysterectomy Infections

During hysterectomy bacteria may enter into the peritoneal cavity through vaginal opening and contaminate the healing tissues. The risk for deep infection after hysterectomy is about 5%. By reducing post-hysterectomy infections, it is possible to reduce individual burden of disease in addition to the direct and indirect financial costs. This study primary aim is to assess if prophylactic preoperative use of azithromycin in addition to generally used cefuroxime decreases post-hysterectomy infections as compared to cefuroxime only prophylaxis during 30 days after hysterectomy. Secondary aim is to assess if there is change in post-hysterectomy superficial infections, urinary tract infections, or post-operative fever between the cohorts and to report possible side-effects of the used antibiotics. In addition, the study finds out a possible role of bacterial vaginosis and microbiome n post-hysterectomy infections.

Participants needed: 2,278
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Helsinki University Central HospitalUpdated: Aug 21, 2024Locations: 6
Eligibility criteria

Women undergoing hysterectomy for benign indication in University Hospitals (Hel...

Inability to understand the study protocol. [+5]

Status: Not yet recruiting

NICU Antibiotics and Outcomes (NANO) Follow-up Study

The NANO follow-up study is designed to determine whether a simple, cost-effective intervention- withholding antibiotics at birth- reduces clinically relevant outcomes such as behavioral and neurological impairment at 2 years of age. This study will be the largest study evaluating the effects of early antibiotics in children with comprehensive measures of neurodevelopment linked to genomic variants and microbiota interactions.

Participants needed: 802
Trial details
Phase: Phase 3Age: 23-30Biological sex: AllType: InterventionalSponsor: Sharp HealthCareUpdated: Aug 4, 2023Locations: 15
Eligibility criteria

Infants at low risk for early onset sepsis-Infants born for maternal indications... [+7]

Status: Recruiting

Preventive Therapy of Postoperative Intra-abdominal Infection Based on Serum Lactate Changes

Intra-abdominal infection is one of the most serious complications after pancreatic resection. The preventive use of antibiotics intraoperatively could reduce the incidence rate of postoperative intra-abdominal infection. According to the previous retrospective study, changes of serum lactate level on postoperative day1 could predict the incidence rate of postoperative intra-abdominal infection. This prospective RCT is to further validate and promote the findings and conclusion.

Participants needed: 297
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Peking Union Medical College HospitalUpdated: Sep 27, 2021Locations: 1
Eligibility criteria

treatment by pancreatic resection, including pancreaticoduodenectomy, pancreatos... [+3]

a history of surgical treatment of any upper abdominal lesions before the curren... [+2]

Status: Recruiting

Prophylactic Oral Antibiotics on Sinonasal Outcomes Following Endoscopic Transsphenoidal Surgery for Pituitary Lesions

To find out whether oral antibiotics given after transsphenoidal endoscopic surgery for pituitary adenoma improves sinus and nasal symptoms, reduces the incidence of infection (sinusitis), and helps mucosal healing in the nasal passages.

Participants needed: 116
Trial details
Phase: Phase 4Age: 18-84Biological sex: AllType: InterventionalSponsor: St. Joseph's Hospital and Medical Center, PhoenixUpdated: Aug 15, 2018Locations: 1
Eligibility criteria

Adult patient undergoing endoscopic surgery for resection of pituitary tumors fo... [+3]

Anaphylaxis/intolerance to the study drugs [+16]